Pharmaceutical Online Videos

  1. Solving Chemistry's Toughest Challenges 7/23/2026

    Discover how Cambrex pairs scientific expertise with collaborative supply chain solutions to turn chemistry's toughest challenges into life-changing therapies.

  2. Learn More About The Data Integration Layer 7/21/2026

    Build a secure, scalable bridge between shop-floor systems and enterprise IT with an integration approach designed for interoperability and future readiness across manufacturing environments.

  3. X-Ray Inspection: Back To The Basics 7/15/2026

    X-ray inspection provides a final quality check after packaging, helping detect missing components, damaged packages, and physical contaminants before products leave the production line.

  4. Metal Detection: Back To The Basics 7/15/2026

    Metal detection helps manufacturers identify contaminants in powders, tablets, and capsules, supporting patient safety, regulatory compliance, reduced waste, and more reliable production.

  5. Check Weighing For Pharmaceuticals: Back To The Basics 7/15/2026

    Dynamic checkweighing helps manufacturers confirm product weight in motion, catch filling errors early, remove noncompliant packages, and support regulatory compliance without interrupting production.

  6. Product Inspection Demo Bus 7/15/2026

    Explore inspection technologies designed to support product quality, regulatory compliance, and production efficiency, with solutions for contaminant detection, connected data management, and more.

  7. Life Changing Products: Modernizing Regulated Product Development And Manufacturing 7/6/2026

    Bridge the gap between your production floor and quality governance. Discover how a unified QMS and MES platform eliminates paper records, automates deviation triggers, and utilizes secure AI tools.

  8. Building A Defensible Visual Inspection Program With Purpose-Built Software 7/6/2026

    Ditch the spreadsheets and de-risk your visual inspection workflow. Learn how purpose-built software automates inspector scheduling and builds a fully defensible, audit-ready cGMP compliance program.

  9. Inline Buffer Formulation Systems 7/6/2026

    Eliminate large storage tanks and optimize cleanroom space with automated inline buffer formulation. See how on-demand fluid handling provides precise, real-time pH and conductivity control.

  10. Optimize Every Step In Your Biopharma Site 7/5/2026

    Bridge the gap between validation and cleanroom execution. Learn how proactive site surveys, residue management, and robust CAPA programs resolve compliance deficiencies and ensure audit readiness.